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| ChemSpiderID=21106337 |
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| SMILES = CCOc1cc(OC)c(cc1OCC)CC(C)N |
| SMILES = CCOc1cc(OC)c(cc1OCC)CC(C)N |
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This article relies largely or entirely on a single source. Relevant discussion may be found on the talk page. Please help improve this articlebyintroducing citations to additional sources.
Find sources: "MEE" psychedelic – news · newspapers · books · scholar · JSTOR (June 2019) |
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Names | |
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IUPAC name
2-(4,5-Diethoxy-2-methoxy-phenyl)-1-methyl-ethylamine | |
Other names
2-Methoxy-4,5-diethoxyphenethylamine | |
Identifiers | |
3D model (JSmol) |
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ChemSpider |
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PubChem CID |
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CompTox Dashboard (EPA) |
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Properties | |
C14H23NO3 | |
Molar mass | 253.342 g·mol−1 |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). |
MEE (2-methoxy-4,5-diethoxyamphetamine) is a lesser-known psychedelic drug of the amphetamine class. It is a diethoxy-methoxy analogofTMA-2. MEE was first synthesized by Alexander Shulgin. In his book PiHKAL, both the dosage and duration are unknown.[1] MEE produces few to no effects. Very little data exists about the pharmacological properties, metabolism, and toxicity of MEE.
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